Some pearl millet-based foods promote satiety or reduce glycaemic response in a crossover trial.


Journal

The British journal of nutrition
ISSN: 1475-2662
Titre abrégé: Br J Nutr
Pays: England
ID NLM: 0372547

Informations de publication

Date de publication:
28 10 2021
Historique:
pubmed: 15 12 2020
medline: 28 1 2022
entrez: 14 12 2020
Statut: ppublish

Résumé

In a previous trial in Mali, we showed that traditional pearl millet couscous and thick porridge delayed gastric emptying (about 5 h half-emptying times) in a normal-weight population compared with non-traditional carbohydrate-based foods (pasta, potatoes, white rice; about 3 h half-emptying times), and in a gastric simulator we showed millet couscous had slower digestion than wheat couscous. In light of these findings, we tested the hypothesis in a normal-weight US population (n 14) that millet foods would reduce glycaemic response (continuous glucose monitor), improve appetitive sensations (visual analogue scale ratings), as well as reduce gastric emptying rate (13C-octanoic acid breath test). Five carbohydrate-based foods (millet couscous - commercial and self-made, millet thick porridge, wheat couscous, white rice) were fed in a crossover trial matched on available carbohydrate basis. Significantly lower overall glycaemic response was observed for all millet-based foods and wheat couscous compared with white rice (P ≤ 0·05). Millet couscous (self-made) had significantly higher glycaemic response than millet couscous (commercial) and wheat couscous (P < 0·0001), but as there were no differences in peak glucose values an extended glycaemic response was indicated for self-made couscous. Millet couscous (self-made) had significantly lower hunger ratings and higher fullness ratings (P < 0·05) than white rice, millet thick porridge and millet couscous (commercial). A normal gastric emptying rate (<3 h half-emptying times) was observed for all foods, with no significant differences among them. In conclusion, some traditionally prepared pearl millet foods show the potential to reduce glycaemic response and promote satiety.

Identifiants

pubmed: 33308328
pii: S0007114520005036
doi: 10.1017/S0007114520005036
doi:

Substances chimiques

Blood Glucose 0

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1168-1178

Auteurs

Anna M R Hayes (AMR)

Whistler Center for Carbohydrate Research & Department of Food Science, Purdue University, West Lafayette, IN, USA.

Fanny Gozzi (F)

Whistler Center for Carbohydrate Research & Department of Food Science, Purdue University, West Lafayette, IN, USA.

Aminata Diatta (A)

Whistler Center for Carbohydrate Research & Department of Food Science, Purdue University, West Lafayette, IN, USA.

Tom Gorissen (T)

The TIM Company, TIM B.V., Zeist, The Netherlands.

Clay Swackhamer (C)

Department of Biological and Agricultural Engineering, University of California, Davis, CA, USA.

Susann Bellmann (S)

The TIM Company, TIM B.V., Zeist, The Netherlands.

Bruce R Hamaker (BR)

Whistler Center for Carbohydrate Research & Department of Food Science, Purdue University, West Lafayette, IN, USA.

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Classifications MeSH